Apicomplexan parasites are attenuated by low-energy electron irradiation in an automated microfluidic system and protect against infection with Toxoplasma gondii

• Published in: Parasitology research (1987) Vol. 122; no. 8; pp. 1819 - 1832
• Main Authors: Finkensieper, Julia, Mayerle, Florian, Rentería-Solís, Zaida, Fertey, Jasmin, Makert, Gustavo R., Lange, Franziska, Besecke, Joana, Schopf, Simone, Poremba, Andre, König, Ulla, Standfest, Bastian, Thoma, Martin, Daugschies, Arwid, Ulbert, Sebastian
• Format: Journal Article
• Language: English
• Published: Berlin/Heidelberg Springer Berlin Heidelberg 01.08.2023; Springer; Springer Nature B.V
• Subjects: Analysis; Animals; Antibodies; Antiparasitic agents; Biomedical and Life Sciences; Biomedicine; Cryptosporidiosis; Cryptosporidium; Electrons; Gamma rays; Immune response; Immunization; Immunology; Intracellular; Medical Microbiology; Mice; Microbiology; Microfluidics; Nucleic acids; Oocysts; Parasites; Protozoa; Radiation; Replication; Scientific equipment and supplies industry; Sporozoites; Tachyzoites; Toxoplasma; Toxoplasma gondii; Wildlife conservation; United States; Germany; Toxoplasma; Irradiation; Cryptosporidium; Attenuation; Vaccine
• ISSN: 0932-0113; 1432-1955
• DOI: 10.1007/s00436-023-07880-w

Radiation-attenuated intracellular parasites are promising immunization strategies. The irradiated parasites are able to invade host cells but fail to fully replicate, which allows for the generation of an efficient immune response. Available radiation technologies such as gamma rays require complex shielding constructions and are difficult to be integrated into pharmaceutical production processes. In this study, we evaluated for the first time low-energy electron irradiation (LEEI) as a method to generate replication-deficient Toxoplasma gondii and Cryptosporidium parvum . Similar to other radiation technologies, LEEI mainly damages nucleic acids; however, it is applicable in standard laboratories. By using a novel, continuous, and microfluidic-based LEEI process, tachyzoites of T. gondii and oocysts of C. parvum were irradiated and subsequently analyzed in vitro. The LEEI-treated parasites invaded host cells but were arrested in intracellular replication. Antibody-based analysis of surface proteins revealed no significant structural damage due to LEEI. Similarly, excystation rates of sporozoites from irradiated C. parvum oocysts were similar to those from untreated controls. Upon immunization of mice, LEEI-attenuated T. gondii tachyzoites induced high levels of antibodies and protected the animals from acute infection. These results suggest that LEEI is a useful technology for the generation of attenuated Apicomplexan parasites and has potential for the development of anti-parasitic vaccines.